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Prazosin Hydrochloride - 0378-3205-01 - (prazosin hydrochloride)

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Drug Information of Prazosin Hydrochloride

Product NDC: 0378-3205
Proprietary Name: Prazosin Hydrochloride
Non Proprietary Name: prazosin hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   prazosin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Prazosin Hydrochloride

Product NDC: 0378-3205
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072575
Marketing Category: ANDA
Start Marketing Date: 20130517

Package Information of Prazosin Hydrochloride

Package NDC: 0378-3205-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-3205-01)

NDC Information of Prazosin Hydrochloride

NDC Code 0378-3205-01
Proprietary Name Prazosin Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-3205-01)
Product NDC 0378-3205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name prazosin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130517
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name PRAZOSIN HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Prazosin Hydrochloride


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